{"orpha":98604,"name":"Congenital alacrima","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-98604/","orphanet_url":"https://www.orpha.net/en/disease/detail/98604","names":{"fr":{"name":"Alacrymie congénitale"},"de":{"name":"Alakrimie, kongenitale"},"es":{"name":"Alacrima congénita"},"it":{"name":"Alacrimia congenita"},"nl":{"name":"Congenitale alacrimie"},"pt":{"name":"Alacrima congénita"},"pl":{"name":"Wrodzony brak łez"},"cs":{"name":"Vrozená alacrima"},"uk":{"name":"Вроджена алакрімія"},"zh":{"name":"先天性无泪症"},"tr":{"name":"Doğumsal alakrima"}},"xrefs":[{"source":"MeSH","code":"C566307","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1863199","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98602,"name":"Rare disorder of the lacrimal apparatus","classifications":[189]},{"orpha":522532,"name":"Rare genetic disorder of the lacrimal apparatus","classifications":[156]}],"children":[{"orpha":404454,"name":"Alacrimia-choreoathetosis-liver dysfunction syndrome","type":"Disease"},{"orpha":86815,"name":"Aplasia of lacrimal and salivary glands","type":"Disease"},{"orpha":1764,"name":"Familial dysautonomia","type":"Disease"},{"orpha":528105,"name":"Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome","type":"Disease"},{"orpha":238468,"name":"Hypohidrotic ectodermal dysplasia","type":"Disease"},{"orpha":98813,"name":"Hypohidrotic ectodermal dysplasia with immunodeficiency","type":"Disease"},{"orpha":289483,"name":"Intellectual disability-alacrima-achalasia syndrome","type":"Disease"},{"orpha":91416,"name":"Isolated congenital alacrima","type":"Disease"},{"orpha":869,"name":"Triple A syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}